Identity
- Trade Name
- BIPOTRODE FDA UDI
- Generic Name
- Endoscopic electrosurgical handpiece/electrode, bipolar, reusable FDA UDI
- Device Name
- ELECTRODE BIPO 5FR TL 360MM for hysteroscopy, PACK=1 PC, for use through a hysteroscope with a 5Fr working channel, reusable FDA UDI
- Model / Reference
- 823005 FDA UDI
- Description
- ELECTRODE BIPO 5FR TL 360MM for hysteroscopy, PACK=1 PC, for use through a hysteroscope with a 5Fr working channel, reusable FDA UDI
Identifiers
- Catalog Number
- 823005 FDA UDI
- Primary DI / UDI-DI
- 04055207000311 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Endoscopic electrosurgical handpiece/electrode, bipolar, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 360 Millimeter FDA UDIOuter Diameter — 1.66666666666 Millimeter FDA UDI
Bipotrode by Richard Wolf GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Richard Wolf GmbH
Sources (1)
- FDA UDI 110f460d-9335-40cb-9013-507319363456 37 fields · synced May 30, 2026